Job Overview The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during
Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve
Experienced Clinical Research Associate, IQVIA Biotech - Home based, Italy 1 day ago Be among the first 25 applicants Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study
Overview In this role you will lead country-level Site Activation activities for Italy, ensuring regulatory compliance and timely delivery of start-up documents. You will act as a single point of contact for investigative sites, SAMs, and
Scope of the Role The IT Engineer – R&D acts as one of the interfaces between the R&D business units and the Global IT organization. This role is responsible for capturing, assessing, prioritizing, and managing business
Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA
Resourcing Life Science is seeking a Clinical Research Associate to monitor phase II-III studies in Italy. The role requires fluency in English and Italian, adherence to GCP, and the ability to initiate and qualify investigators and sites
Legal Associate - M&A, R&D & Procurement Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100
Associate Medical Director, Cardiology, with Metabolic Diseases and Nephrology Experience The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned
The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery
# Associate Medical Director, Cardiology , with Metabolic Diseases and Nephrology ExperienceApplylocations: Milan, Italy: Rome, Italytime type: Full timeposted on: Posted Yesterdayjob requisition id: R1556339 Job Overview The Associate Medical Director will provide medical, clinical and scientific advisory
Experteer Overview In this role, you drive growth for Lonza’s Drug Product Services (DPS) across the EMEA region by acquiring new business and expanding existing accounts. You will collaborate with Business Development, Global Sales, Account Management,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as Associate Feasibility Strategist– Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 Biotechs, spanning 2,700 clinical
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life
Overview The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during the
Senior Associate, IT R&D Engineer Location: Milano, LOM, IT Posted: Jul 21, 2026 Scope of the Role The IT Engineer – R&D acts as one of the interfaces between the R&D business units and the Global IT
The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities, while ensuring
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in our Milan office. Clinical Trial Managers with expertise in
Job Overview Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Italy, particularly in our Milan office. Clinical
Production Manager Responsible for leading and optimizing all manufacturing activities within the plant, ensuring production targets are achieved safely, efficiently, and in compliance with GMP, quality, and regulatory requirements. This role drives operational excellence, continuous improvement,